Gene: [11q24/KCNJ1] potassium inwardly-rectifying channel, subfamily J, member 1; Bartter syndrome, type 2 (antenatal hypercalciuric; MIM:601678); hyperprostaglandin E syndrome (MIM:601678);
REL | See FAM:KCN/00.0. |
REF | CLO,LOC "Krishnan SN &: Hum Genet, 96, 155-160,
1995 CLO,SEQ,STR "Shuck ME &: JBC, 269, 24261-24270, 1994 MUT,HET "Simon DB &: Nature Genet, 14, 152-156, 1996 CLO,SEQ,LOC "Yano H &: Mol Pharmacol, 45, 854-860, 1994 |
SWI | SWISSPROT: P48048 |
KEY | neu, mem, ion, sign |
CLA | coding, basic |
LOC | 11 q24 |
MIM | MIM: 600359 |
